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RNA Docking and Local Translation Regulate Site-Specific Axon Remodeling In Vivo

Published version
Peer-reviewed

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Authors

Holt, CE 
Wong, H-W 
Roque, CG 

Abstract

Nascent proteins can be positioned rapidly at precise subcellular locations by local protein synthesis (LPS) to facilitate localized growth responses. Axon arbor architecture, a major determinant of synaptic connectivity, is shaped by localized growth responses, but it is unknown whether LPS influences these responses in vivo. Using high-resolution live imaging, we examined the spatiotemporal dynamics of RNA and LPS in retinal axons during arborization in vivo. Endogenous RNA tracking reveals that RNA granules dock at sites of branch emergence and invade stabilized branches. Live translation reporter analysis reveals that de novo ß-actin hotspots colocalize with docked RNA granules at the bases and tips of new branches. Inhibition of axonal ß-actin mRNA translation disrupts arbor dynamics primarily by reducing new branch emergence and leads to impoverished terminal arbors. The results demonstrate a requirement for LPS in building arbor complexity and suggest a key role for pre-synaptic LPS in assembling neural circuits.

Description

Keywords

FRAP, RNA labeling, RNA localization, RNA trafficking, axon branching, axon guidance, local protein synthesis, mitochondria, neural wiring, retinotectal projection, β-actin, Actins, Animals, Anisomycin, Axons, Biotin, Blastomeres, Carbocyanines, Cycloheximide, Deoxyuracil Nucleotides, Embryo, Nonmammalian, Gene Expression Regulation, Developmental, In Vitro Techniques, Luminescent Proteins, Mitochondria, Morpholinos, Oligonucleotides, Antisense, Organ Culture Techniques, Protein Synthesis Inhibitors, RNA, Retina, Xenopus laevis

Journal Title

Neuron

Conference Name

Journal ISSN

0896-6273
1097-4199

Volume Title

95

Publisher

Elsevier
Sponsorship
Wellcome Trust (085314/Z/08/Z)
European Research Council (322817)
Wellcome Trust (100329/Z/12/Z)
Wellcome Trust (089703/Z/09/Z)
Biotechnology and Biological Sciences Research Council (BB/H023917/1)
Engineering and Physical Sciences Research Council (EP/H018301/1)
Medical Research Council (MR/K02292X/1)
Medical Research Council (G0902243)
Medical Research Council (MR/K015850/1)
This work was supported by Cambridge Trust, Croucher Foundation, Sir Edward Youde Memorial Fund (H.H.-W.W.), Gates Cambridge (J.Q.L.), Fundac¸ a˜ o para a Cieˆ ncia e Tecnologia (C.M.R.), Wellcome Trust Senior Investigator Award (100329/Z/ 12/Z) (W.A.H.), EPSRC Grant (EP/H018301/1), MRC Grant (MR/K015850/1 and MR/K02292X/1), Wellcome Trust (089703/Z/09/Z) (C.F.K.), Wellcome Trust Programme Grant (085314/Z/08/Z), and ERC Advanced Grant (322817) (C.E.H.).